Hosted on MSN1mon
Some schizophrenia cases stem from malformations of the skull, study suggests
a chromosomal disorder in which one copy of chromosome 22 is missing a small chunk. (Humans typically carry 23 pairs of chromosomes, including one copy of chromosome 22 from each parent.) ...
Nature4y
Chromosomes 15 and 22: deletions and inverted duplication chromosomes
is associated with an abnormal phenotype (the central two are normal chromosome 15). d) The inv dup (22) (right) is associated with the cat eye syndrome.
Nature10d
22q11.2 Deletion Syndrome and Associated Disorders
22q11.2 Deletion Syndrome (22q11.2DS) is a genetic disorder caused by the deletion of a small segment of chromosome 22. This condition is associated with a range of physical, cognitive ...
Hosted on MSN18d
Team links gene duplications, deletions within chromosome region to nonsyndromic bicuspid aortic valve disease
DiGeorge syndrome, a 22q11.2 deletion syndrome, is caused when a small portion of chromosome 22 is missing. The condition can occur in individuals born from a parent with the dominant contiguous ...
Medical Xpress on MSN11d
Mom's X chromosome could speed up brain aging, study suggests
The discovery, which appears Jan. 22 in Nature, could explain the variation ... and women born with just one X chromosome (a ...
Science Daily19d
Link between gene duplications and deletions within chromosome region and nonsyndromic bicuspid aortic valve disease
DiGeorge syndrome, a 22q11.2 deletion syndrome, is caused when a small portion of chromosome 22 is missing. The condition can occur in individuals born from a parent with the dominant contiguous ...